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how_to:web:quantitationresults [2015/07/22 15:59]
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 ====== Quantitation Summary ====== ====== Quantitation Summary ======
- 
-{{ :​how_to:​web:​quanti_summary.png?​direct |}} 
  
 This panel is a summary of your experimental design, listing your biological groups, their samples and their technical replicates. This panel is a summary of your experimental design, listing your biological groups, their samples and their technical replicates.
  
 It also provides the "​Profile Analysis"​ tool you need to launch in order to get Ratio informations and data to be exported. ​ It also provides the "​Profile Analysis"​ tool you need to launch in order to get Ratio informations and data to be exported. ​
 +
 +{{ :​how_to:​web:​dse_quant_results_summary.png?​nolink |}}
 +
 +----
  
 ====== Proteins ====== ====== Proteins ======
  
-{{ :​how_to:​web:​quanti_proteines.png?direct ​|}}+{{ :​how_to:​web:​dse_quant_results_proteins.png?nolink ​|}}
  
-This panel show all the data about the quantified proteins. ​**In order to see the ratio values, you have to launch ​the Profile Analysis from the Summary Panel.**+This panel show all the data about the quantified proteins. ​By default, proteins are groupedbut you can undo it by clicking ​the icon circled in green in the previous screenshotThe view will then be:
  
-Double-clicking a Protein will open its summary panel +{{ :how_to:​web:​dse_quant_results_proteins_ungrouped.png?​nolink |}}
  
-{{ :how_to:​web:​protein_summary.png?​direct |}}+This grid is also provided a filter tool, that you can use as follows:
  
-On this panel, you get an insight of all quantified peptides for this protein. You can click on "Raw XIC" to access the XIC viewer of one Peptide ​.+{{ :​how_to:​web:​dse_quant_results_proteins_filters.png?nolink |}}
  
-{{ :how_to:​web:​quanti_peptide_xic.png?​direct |}}+Double-clicking a Protein will open the //Protein details// panel 
  
 +=== Protein details panel ===
  
 +{{ :​how_to:​web:​protein_quanti_details.png?​direct |}}
 +
 +On this panel, you get an insight of all quantified peptides for this protein (double click on the peptide in the '​Quantified Peptides'​ table or expand directly the peptide panel).
 +
 +{{ :​how_to:​web:​peptide_quanti_details.png?​direct |}}
 +
 + You can click on the eye icon (circled in green) to access the Speclight viewer of this Peptide .
 +
 +TODO: insert link to Speclight doc
 +
 +----
  
 ====== Peptides ====== ====== Peptides ======
  
-{{ :​how_to:​web:​quanti_peptides.png?direct ​|}}+{{ :​how_to:​web:​dse_quant_results_peptides.png?nolink ​|}} 
 + 
 +This is the list of all quantified peptides.  
 + 
 +  * Click on a peptide to see its Master Quant Peptide Ions in the dedicated table below. 
 +  * Double-click on a peptide to open the panel for the feature corresponding to this peptide (see [[#LC-MS Features |LC-MS Features]]).
  
-This is the list of all quantified peptides. Double-clicking on one of them will open the panel for the feature corresponding to this peptide ​(see below).+Note that the peptide ​grid has got a filter tool too.
  
 ====== LC-MS Maps ====== ====== LC-MS Maps ======
  
-This panel offers two tabs to give you informations ​about the Lc-Ms maps of the experiment.  +This panel offers two tabs to give you information ​about the LC-Ms maps of the experiment.
-Click on one or many raw files to display their Lc-Ms map features.+
  
-{{ :​how_to:​web:​quanti_lcms_maps.png?​direct |}}+==== Map alignments ====
  
-The "Map alignment"​ tab shows a chart describing ​the map alignment ​correction performed by Proline for the analysis.+** IMPORTANT: it is crucial to visit this graphics to manually control ​the processed ​map alignments. 
 +A bad alignment ​(showing many curve trends, or too large time deltas) will lead to quantitation errors.** 
 +If you have the feeling that the alignment needs improvement,​ re-run the quantitation,​ tunning the //Alignment Computation//​ part of the //LFQ Params// tab (see [[how_to:​web:​createquantitation|how to create a quantitation]]).
  
-{{ :​how_to:​web:​quanti_map_align.png?direct ​|}}+{{ :​how_to:​web:​dse_quant_results_maps_alignment.png?nolink ​|}}
  
 +On this chart, you can see all the delta time of each LC-MS map against the reference LC-MS map. The reference map is the one specified in the title of the chart. It corresponds to the x axis.
 +
 +==== LC-MS maps 2D viewer ====
 +  ​
 +Click on one or many raw files to display their LC-Ms map features.
 +
 +{{ :​how_to:​web:​dse_quant_results_maps_2d.png?​nolink |}}
 +
 +----
  
 ====== LC-MS Features ====== ====== LC-MS Features ======
  
-This panel lists all the features detected and processed by Proline. ​By clicking one of them, you can see the corresponding XIC on the right-side panel.+This panel lists all the features detected and processed by Proline.\\ 
 +Click a **master feature** to see
 +the corresponding XIC on the right-side panel 
 +- the corresponding features in each file in the bottom grid (first tab) 
 +- the corresponding master quant. peptide ion in the bottom gris (second tab).
  
-{{ :​how_to:​web:​quanti_lcms.png?direct ​|}}+You can double click an entry in the bottom grid to open a dedicated tab (feature/​peptide ion details). 
 + 
 +{{ :​how_to:​web:​dse_quant_results_features.png?nolink ​|}} 
 + 
 +----
  
 ====== LC-MS Peaks ====== ====== LC-MS Peaks ======
  
-All the peaks are listed here, independently from the features they'​ve been gathered to.  +All the peaks are listed here, independently from the features they'​ve been gathered to.
-Click on a Lc-Ms Map name to list all its peaks. By clicking on a peak you can see its XIC charts in the "XIC Viewer"​ at the bottom of the table, or you can double-click it to open the Xic Viewer in a new tab.+
  
-{{ :​how_to:​web:​quanti_peaks.png?direct |}}+Click on a LC-MS Map to list all its peaks in the center grid. Note that this grid is provided a filtering tool.
  
 +Click on a peak (center grid) to see its feature and XIC charts in the bottom panel.
 +You can alternatively double-click a peak to open the XIC Viewer in a new tab.
 +
 +{{ :​how_to:​web:​dse_quant_results_peaks.png?​nolink |}}
 +
 +----
  
 ====== Quantitation Stats ====== ====== Quantitation Stats ======
  
-This tab offers many panel to help you vizualise statistics about your quantitation.+==== Post Processing ====
  
-The first one is a volcano chart of your Proteins based on their -Log10 T-Test P-Value over Log2 Ratio.+{{ :​how_to:​web:​dse_launch_post_processing.png?​350|}} 
 +**In order to see the statistics on the ratios, you have to launch the Post Processing (previously called //Profile Analysis//​).** Launch it from the //Summary// tab toolbar, or from the quantitation node (in project tree) context menu. 
 + 
 +You can see the //Post Processing//​ configuration window below.\\ 
 +See [[prolineconcepts:​lcmsquantitationadvancedconfig| more details on the post-processing parameters]].\\ 
 +Launch the post processing by clicking //Run//. You can watch the task progression in the //Tasks// window. You will also be notified when the task is done. You can then watch the results in the //​Quantitation Stats// tab. 
 + 
 +{{ :​how_to:​web:​dse_post_processing.png?​nolink |}} 
 + 
 +==== Quantitation Statistics ==== 
 + 
 +This tab offers many panel to help you visualize statistics about your quantitation. 
 + 
 +=== Proteins volcano plot === 
 + 
 +The first panel is a volcano chart of your Proteins based on their -Log10 T-Test P-Value over Log2 Ratio. 
 + 
 +{{ :​how_to:​web:​dse_quant_results_protein_volcano.png?​nolink |}}
  
 The Left grid shows a list of all the proteins, and if they are in the actual boudaries of the selection/​exclusion tool. The Left grid shows a list of all the proteins, and if they are in the actual boudaries of the selection/​exclusion tool.
  
-The "AC Filters" ​let you select a color (by clicking on it) and enter an Accession Number (or a part of it) to highlight matching proteins on the chart).+Hover a dot to see information on the protein.\\ 
 +Click on it to open its [[#Protein details panel|protein details panel]]. 
 + 
 +The //AC Filters// let you select a color (by clicking on it) and enter an Accession Number (or a part of it) to highlight matching proteins on the chart). In this example, all proteins containing "​HUMAN"​ in their accession number are colored in orange. By defaults, dots are light blue. 
 + 
 +The //Log2 Fold Change// (of the ratios) and //P-Value// fields let you define new boundaries for the protein selection/​exclusion. It's show on the chart with black lines and gray points to show excluded proteins
  
-The "​Ratio"​ et "​P-Value"​ let you define new boundaries for the protein selection / exclusion. It's show on the chart with black lines and gray points to show excluded proteins+{{ :​how_to:​web:​dse_quant_results_protein_volcano_filtered.png?nolink |}}
  
-{{ :​how_to:​web:​quanti_volcano_prot.png?direct |}}+Select a zone with the mouse cursor to zoom on it. 
 +Use the icon at the top-right of the volcano plot to export it at several picture formats.
  
-The second tab offers the same volcano ​chart for peptides, and you can highlight them with a sequence or ptm definition ​+=== Peptides ​volcano ​plot ===
  
-{{ :​how_to:​web:​quanti_volcano_pep.png?direct |}}+The second tab offers the same volcano chart and options for peptides. Instead of accession number, you can color the dots according to their sequence or PTM definition.
  
 +{{ :​how_to:​web:​dse_quant_results_peptide_volcano.png?​nolink |}}
  
how_to/web/quantitationresults.1437573559.txt.gz · Last modified: 2015/07/22 15:59 by 193.48.0.3